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ETM2

Introduction: ETM2

Description of ETM2

ETM2 (medical condition): An inherited movement disorder involving tremors. Any kind of...more »

See also:

Tremor hereditary essential, 2:
  »Introduction: Tremor hereditary essential, 2
  »Symptoms of Tremor hereditary essential, 2

ETM2: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

ETM2 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that ETM2, or a subtype of ETM2, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

ETM2 as a Disease

ETM2: Another name for Tremor hereditary essential, 2 (or close medical condition association).
  »Introduction: Tremor hereditary essential, 2
  »Symptoms of Tremor hereditary essential, 2

ETM2: Related Diseases

ETM2: ETM2 is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of ETM2 (Tremor hereditary essential, 2)

Some of the symptoms of ETM2 incude:

ETM2: Related Disease Topics

These medical disease topics may be related to ETM2:

Terms associated with ETM2:

Terms Similar to ETM2:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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